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Biotin-PEG2-azide Biotin-PEG2-azide is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Biotin-PEG2-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. Uses: Scientific research. Group: Signaling pathways. CAS No. 1910803-72-3. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-126957. MedChemExpress MCE
Biotin-PEG2-azide Biotin-PEG2-azide is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Biotin-PEG2-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Synonyms: 1H-Thieno[3,4-d]imidazole-4-pentanamide, N-[2-[2-(2-azidoethoxy)ethoxy]ethyl]hexahydro-2-oxo-. CAS No. 1910803-72-3. Molecular formula: C16H28N6O4S. Mole weight: 400.50. BOC Sciences
(+)-Biotin-PEG2-azide (+)-Biotin-PEG2-azide. Group: Polymers. CAS No. 945633-30-7. Product ID: 5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]-N-[2-[2-(2-azidoethoxy)ethoxy]ethyl]pentanamide. Molecular formula: 400.5g/mol. Mole weight: C16H28N6O4S. C1C2C (C (S1)CCCCC (=O)NCCOCCOCCN=[N+]=[N-])NC (=O)N2. InChI=1S / C16H28N6O4S / c17-22-19-6-8-26-10-9-25-7-5-18-14 (23) 4-2-1-3-13-15-12 (11-27-13) 20-16 (24) 21-15 / h12-13, 15H, 1-11H2, (H, 18, 23) (H2, 20, 21, 24) / t12-, 13-, 15- / m0 / s1. OVEZMVONEJMGLZ-YDHLFZDLSA-N. Alfa Chemistry Materials 4
UV Cleavable Biotin-PEG2-Azide UV Cleavable Biotin-PEG2-Azide is a biotin linker. The azide group can react with either alkyne moiety in Cu(I)-catalyzed Click Chemistry reaction or DBCO moiety in copper-free Click Chemistry reaction to form a stable triazole linkage. The hydrophilic PEG spacer increases solubility in aqueous media of the molecules conjugated to the biotin compound. Captured target can be released under mild photolysis conditions (365 nm) and results in a significant decrease of background signal due to non-specifically bound proteins. Please contact us for GMP-grade inquiries. Synonyms: [2-[2-[2-[2-[2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]ethoxy]ethoxy]ethylamino]-2-oxoethoxy]-6-phenacylphenyl] 6-azidohexanoate; 1654739-36-2. Grade: 0.98. CAS No. 1654739-36-2. Molecular formula: C38H51N7O9S. Mole weight: 781.9. BOC Sciences

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